Ds. Thomas et Dw. Turner, LEAF GAS-EXCHANGE OF DROUGHTED AND IRRIGATED BANANA CV WILLIAMS (MUSASPP.) GROWING IN HOT, ARID CONDITIONS, Journal of horticultural science & biotechnology, 73(3), 1998, pp. 419-429
Leaf gas exchange (LGE) of banana plants cv. Williams growing in an ar
id tropical environment was measured on irrigated and droughted plants
through an 8 d drying cycle and after re-irrigation. The relations be
tween net photosynthesis (P-n), stomatal conductance (g(s)), transpira
tion (E-t) and internal CO2 concentration (C-i) and climatic factors (
photosynthetic photon flux density (PPFD), leaf temperature (T-1) and
leaf-to-air vapour pressure difference (Delta e) and plant and soil wa
ter status were explored. The highest P-n, of 23 mu mol CO2 m(-2) s(-1
) and g(s) of 600 mmol m(-2) s(-1), occurred in early to mid morning b
ut the highest E-t, of 10 mmol H2O m(-2) s(-1), occurred in the early
afternoon. Water deficit significantly (P less than or equal to 0.05)
reduced LGE when soil water potential (Psi(S)) at 30 cm soil depth was
less than -30 kPa. The Psi(S) of irrigated plants was maintained abov
e -20 kPa throughout the experiment. Water use efficiency was not sign
ificantly (P less than or equal to 0.05) different between treatments.
Nor was the relation between the difference between leaf and air temp
erature (T-d) and Delta e. A unique relation existed between P-n and g
(s) that was common to both irrigated and droughted plants. Soil droug
ht, and in irrigated plants diurnal variation in Delta e and T-1, redu
ced P-n and g(s). C-i was positively correlated with both P-n and g(s)
except when the plants had experienced more than 6 d of drought (Psi(
S) lower than -50 kPa) when the relations became non-significant (P le
ss than or equal to 0.05). After re-irrigation of the droughted plants
these relations returned to being positive and statistically signific
ant (P less than or equal to 0.05). Measurements of leaf water potenti
al using either volumetric or pressure techniques rarely showed differ
ences between irrigated and droughted plants. This was despite a large
reduction in P-n, E-t and g(s). Mature banana leaves folded their lam
inae to a greater extent, and for longer periods during the day, in dr
oughted plants but we suggest leaf folding may be too variable over th
e diurnal period to be used as a plant-based indicator of water defici
t. The youngest leaf emerged up to 40% faster during the night than th
e day suggesting that day temperatures were above the optimum for leaf
elongation. Drought significantly (P less than or equal to 0.05) redu
ced elongation of emerging leaves only when Psi(S) was less than -65 k
Pa. In irrigated plants P-n was reduced whenever g(s) declined due to
diurnal changes in the environment. Psi(S) less than -30 kPa further r
educed LGE in droughted plants but few associations with plant water s
tatus (either pressure or volume based measurements of leaf water stat
us or plant morphology) could be linked with decreased LGE. We conclud
e that banana plants are well able to maintain their internal water st
atus during drought and are sensitive to soil drying. Water status is
maintained by reducing radiation load (leaf folding) and closing stoma
ta. This is likely to bear strongly on the productivity of this crop i
n hot, arid environments.